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For: Sielemann K, Elbeck Z, Gärtner A, Brodehl A, Stanasiuk C, Fox H, Paluszkiewicz L, Tiesmeier J, Wlost S, Gummert J, Albaum SP, Sielemann J, Knöll R, Milting H. Distinct Myocardial Transcriptomic Profiles of Cardiomyopathies Stratified by the Mutant Genes. Genes (Basel) 2020;11:E1430. [PMID: 33260757 DOI: 10.3390/genes11121430] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
Number Citing Articles
1 Zhang Y, Xie J, Wu Y, Zhang B, Zhou C, Gao X, Xie X, Li X, Yu J, Wang X, Cheng D, Zhou J, Chen Z, Fan F, Zhou X, Yang B. Novel algorithm for diagnosis of Arrhythmogenic cardiomyopathy and dilated cardiomyopathy: Key gene expression profiling using machine learning. J Gene Med 2023;25:e3468. [PMID: 36518003 DOI: 10.1002/jgm.3468] [Reference Citation Analysis]
2 Koslow M, Mondaca-Ruff D, Xu X. Transcriptome studies of inherited dilated cardiomyopathies. Mamm Genome 2023. [PMID: 36749382 DOI: 10.1007/s00335-023-09978-z] [Reference Citation Analysis]
3 Elbeck Z, Hossain MB, Siga H, Oskolkov N, Karlsson F, Lindgren J, Walentinsson A, Remedios CD, Koppenhöfer D, Jarvis R, Bürli R, Jamier T, Franssen E, Firth M, Degasperi A, Bendtsen C, Dudek J, Kohlhaas M, Nickel AG, Lund LH, Maack C, Végvári Á, Betsholtz C. Epigenetic modulators link mitochondrial redox homeostasis to cardiac function.. [DOI: 10.1101/2022.03.26.485908] [Reference Citation Analysis]
4 Fomin A, Gärtner A, Cyganek L, Tiburcy M, Tuleta I, Wellers L, Folsche L, Hobbach AJ, von Frieling-Salewsky M, Unger A, Hucke A, Koser F, Kassner A, Sielemann K, Streckfuß-Bömeke K, Hasenfuss G, Goedel A, Laugwitz KL, Moretti A, Gummert JF, Dos Remedios CG, Reinecke H, Knöll R, van Heesch S, Hubner N, Zimmermann WH, Milting H, Linke WA. Truncated titin proteins and titin haploinsufficiency are targets for functional recovery in human cardiomyopathy due to TTN mutations. Sci Transl Med 2021;13:eabd3079. [PMID: 34731013 DOI: 10.1126/scitranslmed.abd3079] [Cited by in Crossref: 17] [Cited by in F6Publishing: 17] [Article Influence: 8.5] [Reference Citation Analysis]
5 Gaertner A, Bloebaum J, Brodehl A, Klauke B, Sielemann K, Kassner A, Fox H, Morshuis M, Tiesmeier J, Schulz U, Knoell R, Gummert J, Milting H. The Combined Human Genotype of Truncating TTN and RBM20 Mutations Is Associated with Severe and Early Onset of Dilated Cardiomyopathy. Genes (Basel) 2021;12:883. [PMID: 34201072 DOI: 10.3390/genes12060883] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
6 Brodehl A, Milting H, Gerull B. Special Issue "Cardiovascular Genetics". Genes (Basel) 2021;12:479. [PMID: 33810227 DOI: 10.3390/genes12040479] [Reference Citation Analysis]